Thermal detection system for failure in electrical apparatus and thermal detecting paint compositions

ABSTRACT

A system for detecting thermal breakdown of organic resin coatings is described which can be used for locating failure occurring in electrical apparatus based on the use of a minor amount of a chemical tagging material. The chemical tag can be readily extracted from particulate generated by the thermal breakdown of the organic resin coating by extracting the particulate with an organic solvent and analyzing the extract in a gas chromatograph using an electron capture detector. Useful results have been found when employing certain halogenated aromatic organic compounds, such as N-alkyl tetrahalophthalimides, which can be employed in the particulating resin at concentrations of as little as 0.01% by weight.

This application is a continuation-in-part application of copending application Ser. No. 806,600, filed June 15, 1977 and Ser. No. 807,067, filed June 16, 1977 and assigned to the same assignee as the present invention. The subject matter of Ser. No. 806,600 and Ser. No. 807,067 is incorporated herein by reference.

The present invention relates to a thermal detection system useful for locating failure in electrical apparatus, such as apparatus useful in generating electric power. More particularly, the present invention relates to the use of certain chemical tagging compounds, such as poly-haloaromatic N-organo substituted phthalimides, which can be employed in extremely low concentrations as finger prints, in organic resin insulating coatings.

U.S. Pat. No. 3,427,880, Grobel et al, assigned to the same assignee as the present invention, for Over Heating Detector For Gas Cooled Electric Machine, shows the use of an ion chamber particle detector for detecting excessive heating of gas cooled components in an electric generator. Local overheating of parts in the stator core of a gas cooled dynamo electric machine, such as the stator laminations, can be detected by the use of an ion chamber particle detector and an indicator for showing the presence of smoke. Certain coating materials, such as polystyrene, polymethylmethacrylate, etc., were suggested as giving advanced warning when temperatures in the range of 230° C. to 240° C. were obtained. It was further suggested that the use of a temperature indicating paint changing color from yellow to brown at 235° C. would allow the operator to locate where the particulate was being generated. A further publication "Immediate Warning of Local Over Heating in Electric Machine by the Detection of Pyrolysis Products", which was presented at the Institute of Electrical and Electronic Engineers, Powder Engineering Society, summer meeting on July 19, 1972, by C. Carson et al, suggested that mass spectrometric analysis and gas chromatographic analysis could be used to indicate the area where local overheating was occurring in electric apparatus by the use of selective coatings. Various pyrolysis products, such as phenolic varnish, epoxy glass pressed composites, silicon rubber, etc., were shown to provide various peaks, based on the use of the mass spectrometer and gas chromatograph. Additional study was required to clearly differentiate and identify particulate arising from gas streams, such as hydrogen or helium used to cool electric apparatus. It was virtually impossible to specifically locate the area from which the particulate was generated in the electric apparatus because of the complexity of the mixture which normally contained a number of background materials continuously generated under normal operating conditions.

Additional investigation of the problem of making compositions useful for forming thermal particulating coatings in electrical apparatus for the purpose of locating local overheating, as shown by Forte et al, U.S. Pat. No. 3,982,225 and Smith et al U.S. Pat. Nos. 3,973,438 and 3,973,439. Particular chemical compounds, such as malonic acid and metal acetyl acetonates, were proposed by Smith et al as compounds to form a thermal particulating coating at a particular temperature, such as 125° C. or 90°-180° C. Concentrations of from 5 parts to 200 parts of the aforementioned compounds, per 100 parts of the resin carrier were suggested. In addition, an organic solvent could also be utilized in the composition. For obvious reasons, it was highly unlikely that such coating materials were feasible under actual operating conditions in electric apparatus, such as turbine generator, which must be maintained in a critical controlled environment, substantially free of contaminants. In "Chemical Monitoring of Hydrogen Cooled Turbine Generators Brought Up To Date", by Sexton et al, Rotating Machinery 42AIC75, Sec. 7-401-7-406, it has been suggested that carefully formulated sacrifical compounds capable of particulating at a temperature of between 100° C. to 130° C. could be employed to give an indication of the specific location within the machine where the overheating is taking place or particulate at a temperature of 70°-100° C. less than the normal organic materials. Efforts to achieve such results, based on the aforementioned guidelines, were unsuccessful because in many instances it was difficult to specifically identify the chemical tagging compounds unless high concentrations were employed to overcome background interference in the particulate which created contamination problems. In addition, if the compound vaporized at too low a temperature, it invariable would be released from the thermal particulating resin coating during extended operation at normal temperatures, based on its volatility. Further, it was difficult to differentiate the sacrificial compounds from other sacrificial compounds where different sacrificial compounds or "tags" were applied over a variety of locations in the electric apparatus.

The present invention is based on the discovery that certain polyhalogenated aromatic compounds or polyfluorinated aliphatic compounds having a chemical decomposition temperature of at least 100° C. higher than the particulating temperature of the thermal particulating temperature of the organic resin matrix material, can be detected at extremely low levels of concentration when utilizing a gas chromatograph equipped with an electron capture detector or a micro coulometric detector.

There is provided by the present invention, a thermal detection system for electrical apparatus, comprising a monitor suitable for detecting smoke particles, a collecting means for removing said smoke particles for analysis and thermal particulating organic resin coated on several surfaces of the electrical apparatus, where a set of at least two different chemical tags are respectively utilized on different surfaces of the electrical apparatus at a concentration in the thermal particulating organic resin coating of from about 0.01% to 0.5% and are characterized by having a volatility range equivalent to a C.sub.(24-45) aliphatic paraffin and are selected from aromatic polychlorinated organic compounds, aromatic polyfluorinated organic compounds and aliphatic polyfluorinated organic compounds capable of resisting chemical decomposition up to temperatures of at least 100° C. greater than the smoking temperature of the thermal particulating organic resin, and where each chemical tag can be readily distinguished from another chemical tag when utilized in the thermal particulating organic resin and collected with the organic resin particulate obtained from the collecting means and analyzed as a solvent extract in a gas chromatograph equipped with an electron capture detector or a micro coulometric detector and identified as a member of the total set of chemical tags utilized in the electrical apparatus to establish the location of the organic resin particulate generated in the electrical apparatus.

The chemical tags which can be used in combination with the thermal particulating organic resin in the practice of the invention, are compounds including aromatic polychlorinated organic compounds, aromatic polyfluorinated organic compounds and aliphatic polyfluorinated organic compounds having a volatility in the range of a C.sub.(24-45) aliphatic paraffin. Among the preferred chemical tagging compounds which can be used in the practice of the present invention are tetrahalophthalamic acids of the formula, ##STR1## tetrahalobenzamides of the formula, ##STR2## and tetrahalophthalimides of the formula, ##STR3## where X is a halogen radical, R and R¹ together total 12-24 carbon atoms and are selected from C.sub.(1-23) alkyl radicals, C.sub.(6-20) cycloalkyl radicals, and divalent heterocyclic radicals, where the divalent heterocyclic radicals joined to N of formula (1) have the formula, ##STR4## Q is selected from --O--, --S-- and --SO₂ -- and y and z are integers having a value of 1 to 23 inclusive while together total 12 to 24; R² and R³ are selected from alkyl and cycloalkyl radicals as previously defined for R and R¹ ; R⁴ is selected from C.sub.(6-20) alkyl and, cycloalkyl.

Radicals included by X of formulas 1-3, are for example, chloro, fluoro, etc.; R-R³ radicals include methyl, ethyl, propyl, butyl, pentyl, etc.; cycloalkyl radicals included jointly by R-R³ are cyclohexyl, cycloheptyl, etc. There are included by R⁴ radicals ethoxypropyl, ethylthiopropyl, ethylsulfone propyl, hexyl, heptyl, octyl, etc.

The tetrahalophthalamic acids of formula (1) can be synthesized by standard procedures from tetrachlorophthalic anhydride and a secondary amine such as diisopropyl amine, dibutyl amine, diamyl amine, dihexyl amine, dicyclohexyl amine, pyrrolidine, morpholine, 2,6-dimethyl morpholine, piperidine. There can be used two equivalents of amine per equivalent of tetrachlorophthalic anhydride in tetrahydrofuran solvent at room temperature.

The tetrahalophthalimides of formula (3) can be made in accordance with standard techniques using tetrahalophthalic anhydride and a primary amine such as hexyl amine, 2-amino-3,3-dimethylbutane, cyclohexyl amine, octyl amine, 2-octyl amine, cyclooctyl amine, dodecyl amine, adamantyl amine, 3-methoxylaminopropane, cyclododecyl amine, cycloheptyl amine, nonyl amine, decyl amine, heptyl amine, etc.

Compounds of formulas (1)-(3 can be utilized as chemical tags in combination with various particulating organic resin compositions, which are capable of smoking at temperatures below 250° C. and which include insulating resin useful for insulating metallic conductors which may or may not be pigmented, or as a paint which can be applied on existing insulating organic resin compositions used for insulating various parts of electric apparatus, such as a wire insulation, stator laminations, etc.

It has been found that a critical relationship exists between the number of carbon atoms present in R-R⁴ of formulas 1-3 as defined above, and the ability of these compounds to serve as chemical tags in the thermal detection system of the present invention. For example, if R⁴ is alkyl and less than six carbon atoms, or the sum of R and R² or R² and R³ respectively is less than twelve carbon atoms, the compounds of formulas 1-3 cannot be identified in the generated particulate.

An important aspect of our invention is the use of a gas chromatograph equippped with a 63 Ni Electron Capture Detector (63 Ni ECD) such as those commercially available from Hewlett Packard and Varian Aerograph. The basic principles of operation of the 63 Ni ECD involves a radioactive foil (63 Ni) which emits particles with a maximum energy of about 67 KeV. As the particles travel through the carrier gas, they ionize the carrier gas (nitrogen or methane-argon) and produce positive ions and secondary electrons. The negative cell voltage applied to the cathode connection cause the secondary electrons (free electrons) to be driven toward the anode connection. The free electrons are collected at the anode and produce a steady background (standing) current. When a sample compound with an affinity for free electrons enters the detector, the standing current is reduced. The amount of reduction is a function of the sample concentration and the electron affinity of the compound. The decrease in standing current is sensed by an electrometer through the anode connection. This signal is them amplified to a sufficient level to operate a potentiometer strip chart.

The drawing shows a gas chromatogram which results from the injection of mixture of a set of tags into the gas chromatograph equiped as described above.

For all practical purposes our invention excludes the elements bromine and iodine as potential halogens for the preparation of tags. This is because both iodine and bromine form organic compounds which even when attached to an aromatic nucleus tend to be unstable as a result of evolution of free halogen at elevated temperatures. In addition, since the sensitivity of the electron capture detector is a function of the number of halogens present, it is much more difficult to achieve high sensitivity with bromine and iodine since their molecular weight renders multiple substituted derivatives unsuitable for gas chromatography due to limited volatility of the derivative.

In general terms, the tag design aspect of our invention consists of any set of two or more halogenated compounds which can be resolved by a gas chromatograph equipped with an electron capture detector, where halogenated means multiply chlorinated or fluorinated and where the boiling point of all members of the set is such that the Kovats Index on OV-17 (phenylmethylpolysiloxane) is between about 2700 and 4500, i.e. comes off a gas chromatograph between a C₂₇ and a C₄₅ hydrocarbon. The Kovats Index, described in detail in a paper by Wehrli and Kovats, Helv. Chim Acta, 42, 2709, (1959), is a retention index and appears to relate to the ability of the tag to be absorbed on the smoke particles. The primary factors are polarity and molecular weight which are also related to the boiling point. It should be noted that other liquid phases, such as OV-1 (dimethylpolysiloxane), can be used and these may provide different resolutions.

Suitable particulating organic resins which can be used in combination with the above chemical tags of formulas 1-3 in the practice of the invention, are pigmented epoxy paints of the Insulating and Laminating Business Department of the General Electric Company, such as (74004) diglycidyl ether of Bisphenol-A used with (74010) amine terminated polyamide hardner. This epoxy paint can be pigmented with various colors. In addition, a water based modified alkyl, Reeves 2968, of the C. A. Reeves Paint Company of Syracuse, New York also can be used. Other organic paints also can be used which can be thermally particulated at temperatures below 250° C., etc.

In the practice of one form of the invention, electric apparatus subject to overheating in particular locations, such as a stator core of a turbine generator, can be painted with a pigmented thermal particulating resin in at least two different locations with a different chemical tag in each location. As used hereinafter, the term "thermal particulating organic resin" will signify a tag containing pigmented coating in an electric apparatus which has been applied onto existing insulation of such electric apparatus.

As described in the above cited publication of Carson et al, "Immediate Warning of Local Overheating in electrical Machines by the Detection of Pyrolysis Products", a typical electric generator powered by a steam turbine can develop local overheating in stator cores, based on damage to the surface of a "tooth". In instances where a thermal condition is created which is capable of causing the smoking of a thermal particulating organic resin, the smoke can be carried to a core monitor using an ionization chamber detector, based on the circulation of hydrogen coolant. A collector is employed to trap the smoke particles for analysis. Removal of the collector and the treatment of the trapped particulate with an organic solvent can provide an extract useful for gas chromatographic analysis. An electron capture detector utilized with the gas chromatograph can readily identify specific chemical tags even at extremely low concentrations, although the particulate consists of a wide variety of pyrolyzed volatiles carried by the hydrogen coolant from throughout the whoe generator. The application of the electron capture detector in Gas-Liquid Chromatography is shown by Martin Scolnick, "The Concentric Cylinder Electron Capture Detector Standing Current Studies in the DC and Pulsed Voltage Modes", Journal of Chromatographic Science, 7, 263 (1969). Also "An Introduction to Separation Science", Barry L. Karger et al, pp. 232-4, John Wiley & Sons, New York (19).

In another aspect of the invention, the electric apparatus can be a combination of wire terminals in a telephone exchange, a power system in a nuclear submarine, a nuclear generator, etc. In instances where circulating gaseous coolant is not used, a smoke detector can be employed to activate a vacuum system to collect particulate which can be then analyzed as previously described. The location of the source of failure can be readily determined by employing the electron capture technique as described above.

In order that those skilled in the art will be better able to practice the invention, the following examples are given by way of illustration and not by way of limitation. All parts are by weight.

EXAMPLE 1

Several mixtures having respectively equal molar amounts of tetrachlorophthalic anhydride and a different primary amine were refluxed in acetic acid under nitrogen over periods of from 2-168 hours. Each mixture was allowed to cool to room temperatures and each of the respective products was allowed to crystallize. The crystalline materials were respectively collected on a filter, washed with water and dried in vacuo resulting in a yield of between 67-68% of the corresponding N-alkyl or N-cycloalkyl tetrachlorophthalimide. The following amines were employed in making the N-alkyl tetrachlorophthalimides by the aforementioned procedures:

    ______________________________________                                                            Imide                                                       Amine              (Melting Point °C.)                                  ______________________________________                                         Ethyl Amine        191.5-195                                                   Isobutyl Amine     178-179.5                                                   Pentyl Amine       147.6-149                                                   Hexyl Amine        150-151.5                                                   2-Amino-3,3-                                                                   dimethyl Butane    165-165.5                                                   Octyl Amine        142-143                                                     Cyclo Octyl Amine  240-207                                                     Dodecyl Amine      135.5-137                                                   Adamantyl Amine    235-238.5                                                   Aniline            273-274                                                     ______________________________________                                    

A second set of compounds or "tags" were synthesized by the following procedure: Two equivalents of a secondary amine were combined with one equivalent of tetrachlorophthalic anhydride in tetrahydrofuran at room temperatures and the mixture was stirred and allowed to stand for 1 hours. The resulting solution was evaporated to dryness and the residue dissolved in water and acidified with HCl. The crystals which separated on acidification were filtered and recrystallized. As the secondary amine, there was employed dihexyl amine and morpholine which respectively formed the corresponding tetrachlorophthalamic acid having a melting point of 113°-114° C. and 111.5°-113° C.

Several paints were respectively prepared by mixing about 100 parts of diglycidyl ether of Bisphenol-A having 73% solids containing about 0.1% by weight of one of the above-identified chemical tags, with 29.43 parts of an amine terminated polyamide amine hardener. The respective paints were then applied to a thickness of 0.01 inch into several 1:×13" nichrome strips which were allowed to cure. The painted nichrome strips were then mounted on a flange with a common center electrode and 9 independent electrodes situated radially about the center. The flange was then mounted onto the main housing in the interior of a large steam turbine-generator. A large electric arc welder power supply (400 amps) was connected to the common central electrode and sequentially to each of the radial electrodes. Current was randomly applied to each of the nichrome strips at intervals of about 20 minutes and maintained for a 5 minute period for each strip to effect the pyrolysis of the resin on the strip. A pyrolysis signal was observed on the core monitor connected to a test operating generator. A portion of hydrogen coolant was then vented through a glass fiber disc. The disc collected the pyrolyzed particulate and the collection continued as long as the signal was being received on the core monitor. During the sampling period, the power was gradually increased through the test strip to insure complete pyrolysis of the sample. After a pyrolysis signal was no longer detected on the core monitor, sampling through the glass filter terminated. At this point, the lead from the power supply, connected to a particular radial electrode, was advanced to another radial electrode in accordance with an arbitrary, but recorded sequence. All of the 9 nichrome strips were sequentially electrically heated to effect the generation of particulate which was collected on respective glass fiber discs. As the glass fiber discs were removed from the collector, they were placed in glass vials, containing methanol, number in the same order the glass fiber discs were removed from the collector. The glass vials were then shaken and the methanol extract was analyzed as described below to determine the presence of a particular N-alkyl tetrachlorophthalimide or benzamide. Identity of a particular tag was confirmed by comparing its elution volume on a gas chromatograph trace of the total set of the N-alkyl phthalimides used in the test.

There was used a Hewlett Packard 5830A Gas Chromatograph equipped with an electron capture detector. The analytical conditions are summarized below:

Column: 6'×0.25" Pyrex packed with 3% OV-17 on gas chromatograph 100-120 mesh

Injector: 300° C.

Detector: 300° C.

Oven: Programmed from 240°-270° C. at 4° min.

Flow: 38 ml/min Argon-Methane

Sample Injection: One microliter injected using a Hamilton 10 microliter syringe

The following results were obtained when the respective particulate extracts were analyzed by the gas chromatograph using the electron capture in accordance with above procedure, where "tag" is expressed in terms of the organic radical attached to the amine used in making either the tetrachlorophthalamic acid or the N-alkyl tetrachlorophthalimide and the term "detected" indicates whether the analysis of the particulate extract using the gas chromatograph and the electron capture detector to determine the presence of the tag in the particulate was effective or not:

    ______________________________________                                         Tag                   Detected                                                 ______________________________________                                         Hexyl                 Yes                                                      Cyclo Octyl           Yes                                                      Dodecyl               Yes                                                      3,3-dimethyl                                                                   2-butyl               No                                                       Pentyl                No                                                       Morpholine            Yes                                                      Isobutyl              No                                                       Ethyl                 No                                                       Methoxy Propyl        Yes                                                      ______________________________________                                    

The above results show that the volatility of the tag in terms of the length of the alkyl chain attached to nitrogen is a significant factor with respect to whether the particular N-alkyl tetrachlorophthalimide or tetrachlorophthalamic acid can be employed as a tag in the practice of the present invention.

In a subsequent run following the same procedure, additional tags were identified, such as adamantyl, and octyl tetrachlorophthalimides and dihexyl tetrachlorobenzamide. The latter resulted from thermal decarboxylation of the corresponding amic acid included by formula (1).

EXAMPLE 2

Various parts of a 496 MVA-2 pole large steam turbine generator are painted with a set of chemical tags in accordance with the procedure of Example 1. More specifically, the epoxy paint of Example 1 is pigmented with various colors, and the pigmented tag containing paints are applied to different parts of the turbine-generator as shown as follows:

    ______________________________________                                                     Chemical Tag                                                                   (Tetrachloro-                                                                               Turbine Generator                                     Color       phthalimide) Part                                                  ______________________________________                                         Pink        N-methoxy-   Turbine end core                                                  propyl                                                             Blue        N-hexyl      Center Core                                           Orange      Dihexyl      Collector & core                                      Yellow      N-heptyl     End winding                                           Green       N-octyl      Lower frame                                                                    extension                                             Red         Cycloheptyl  Reactor                                               Dark Blue   Cyclooctyl   Transformer                                           Light Blue  Dodecyl      Rotor                                                 ______________________________________                                    

Under normal operation, the above generator is enclosed in a hydrogen atmosphere at a pressure of about 48 psi. During operation a thermal breakdown occurs and the core monitor alarm sounds. A sample of the particulate generator as a result of the breakdown is automatically collected on a glass fiber disc. The generator is then shut down. The glass fiber disc is removed and placed in a vial containing methanol.

The methanol extract is injected into a Hewlett-Packard 5830A Gas Chromatograph equipped with an electron capture detector in accordance with the procedure of Example 1. When the elution volume of the sample is compared to the total trace of a tag set shown in the Table below and in the Figure, it is found that N-hexyl tetrachlorophthalimide is present in the particulate. This establishes that the breakdown occurs in the center core of the large steam turbine-generator. An investigation confirms the breakdown and appropriate maintenance is initiated.

    ______________________________________                                                 (Peak-)   (Total)                                                      RT (min)                                                                               Area      Area %    ECD Interpretation                                 ______________________________________                                         3.27    2298000   7.759     N-methoxypropyl                                                                tetrachlorophthalimide                             3.61    2619000   8.843     N-hexyl                                                                        tetrachlorophthalimide                             4.08    2258000   7.624     N,N-dihexyl                                                                    tetrachlorobenzamide                               4.38    8978000   30.315    N-heptyl                                                                       tetrachlorophthalimide                             5.25    1489000   5.028     N-octyl                                                                        tetrachlorophthalimide                             6.37    2632000   8.887     N-cycloheptyl                                                                  tetrachlorophthalimide                             7.83    2365000   7.986     N-cyclooctyl                                                                   tetrachlorophthalimide                             9.80     932200   3.148     N-dodecyl                                                                      tetrachlorophthalimide                             11.94   2321000   7.837     N-adamantyl                                                                    tetrachlorophthalimide                             13.77   3493000   11.794    N-cyclododecyl                                                                 tetrachlorophthalimide                             ______________________________________                                    

EXAMPLE 3

In accordance with the procedure of Example 1, three nichrome wire samples were painted with the epoxy paint of Example 1 which contained about 0.1% of each of the following tags which are expressed in terms of the N-organo radical of either the tetrachlorophthalamic acid or an N-alkyl tetrachlorophthalimide as shown in Example 1, such as methoxy propyl, N-hexyl, dihexyl, N-heptyl, N-octyl, cyclo-heptyl, cyclo-octyl, dodecyl, adamantyl, and cyclo-dodecyl. The paint containing the aforementioned mixture of tags was applied onto plain nichrome wire and also nichrome wire having a polyvinylchloride insulation. The nichrome wire was then heated using about 10 V from a 110 volt AC variac. Smoke was collected in air using a glass filter using a gentle stream of air passing through a glass tube which had the wire positioned at one end and the glass filter at the other end. Following the procedure of Example 1, the extract of the particulate collected on the glass filter was analyzed with a gas chromatograph using an electron capture detector. It was found that all of the 10 tags were readily identified in the three wire samples. This demonstrates that the tags survive pyrolysis in an air atmosphere.

Although the above examples are directed to only a few of the very many chemical tags and thermal particulated organic resins which can be used in combination with such tags in the practice of the present invention, it should be understood that the present invention is directed to the use of a much broader variety of chemical tags and such thermal particulating organic resins. For example, the term "aliphatic polyfluorinated organic compound" includes compounds having the following formula, ##STR5## where n is an integer from 1 to 12 inclusive and R⁷ is selected from C.sub.(1-20) alkyl and cycloalkyl radicals, where the volatility of the compounds of formula (4) are as previously defined. In addition to electric generators, the system of the present invention can be applied to control cable bundles in a nuclear power plant, telephone exchange-switching complexes, electric motors, etc. 

What we claim as new and desire to secure by Letters Patent of the United States is:
 1. In a method for locating failure in electrical apparatus to prevent thermal damage in such electrical apparatus based on the use of a monitor suitable for detecting smoke particles arising from the thermal breakdown of an organic resin, a collecting means for accumulating said smoke particles, and an analytical means to determine the location of electrical failure based on an analysis of the smoke particulate, whereby uncertainty of the location of the electrical failure results due to the difficulty of clearly distinguishing the particulate arising from normal background electrical apparatus operation, from particulate arising from the site of electrical failure, the improvement which comprises,(1) coating the electrical apparatus in at least two principal locations with thermal particulating organic paint compositions comprising a thermal particulating organic resin having a smoking temperature below 250° C. and a member of a set of identifying chemical tags resulting respectively in the deposition of a chemical tag for each preselected surface of the electrical apparatus, (2) and when smoking occurs as a result of electrical breakdown, collecting organic resin particulate obtained from the collecting means and analyzing it as a solvent extract in a gas chromatograph equipped with an electron capture detector or a micro coulometric detector whereby a member of the total set of chemical tags utilized in the electric apparatus can be identified to establish the location of the organic resin particulate generated in the electrical apparatus, and the difficulty in establishing the respective chemical tags from background organic resin particulate is overcome, where each chemical tag is used in the paint composition at from about 0.01 percent to 0.5 percent by weight of the paint composition and characterized by having a volatility range equivalent to a C(24-45) aliphatic paraffin and selected from the class consisting of(A) chemical tags selected from halogenated aromatic organic compounds and polyfluorinated aliphatic organic compounds capable of resisting decomposition at temperatures at least 100° C. higher than the smoking temperature of the thermal particulating organic resin and (B) chemical tags in the form of halogenated aromatic amic acids which are convertible to halogenated aromatic organic compounds of (A) at smoking temperatures.
 2. A method in accordance with claim 1 where the chemical tags are organic compounds having the formula, ##STR6## where X is a halogen radical, R and R¹ are separately selected from C.sub.(1-23) alkyl radicals, which together total C.sub.(12-24) carbon atoms, C.sub.(6-20) cycloalkyl radicals and heterocyclic radicals, where the valence of the nitrogen atoms can be satisfied with a heterocyclic radical having the formula, ##STR7## Q is selected from --O--, --S-- and --SO₂ -- and y and z are integers having a value of 1 to 23 inclusive while together total 12 to
 24. 3. A method in accordance with claim 1 where the chemical tags are organic compounds having the formula, ##STR8## where X is a halogen radical, R² and R³ are separately selected from C.sub.(1-24) alkyl radicals, which together total C.sub.(12-24) carbon atoms and C.sub.(6-20) cycloalkyl radicals.
 4. A method in accordance with claim 1, where the chemical tags are organic compounds having the formula, ##STR9## where X is a halogen radical and R⁴ is selected from C.sub.(6-20) alkyl, and cycloalkyl.
 5. In a method of detecting overheating in an electric machine having cooling gas recirculating over parts subject to overheating while the machine is operation, said machine having a coating composition on said parts selected to produce submicron particles from a thermal particulating organic resin on reaching a temperature below 250° C., a portion of said cooling gas being extracted from the machine and monitored for the presence of said particles to detect overheating, the improvement comprising(1) incorporating in said coating composition 0.01 to 0.50 percent by weight a set of chemical tagging compounds selected from the group consisting of an organic compound of the formula, ##STR10## an organic compound of the formula, ##STR11## and an organic compound of the formula, ##STR12## (2) collecting the sub-micron particles, (3) extracting the sub-micron particles in an organic solvent, and (4) using a gas chromatograh equipped with an electron capture detector to detect the tags in the organic solvent extract, where X is a halogen radical, R and R¹ together total 12-24 carbon atoms and are selected from C.sub.(1-23) alkyl radicals, C.sub.(6-20) cycloalkyl radicals and divalent heterocyclic radicals, where the valence of the nitrogen atoms can be satisfied with a heterocyclic radical having the formula, ##STR13## Q is selected from --O--, --S-- and --SO₂ -- and y and z are integers having a value of 1 to 23 inclusive while together totaling 12 to
 24. 6. The method of claim 5, wherein the set of tagging compounds is selected from the group consisting of halogenated imide and halogenated amic acid.
 7. The method of claim 5, wherein said tagging compounds for application of separate designated portions of the machine consist essentially of:N,N-dihexyl tetrachlorophthalimic acid, N-hexyl tetrachlorophthalimide, N-octyl tetrachlorophthalimide, N-cyclooctyl tetrachlorophthalimide, N-dodecyl tetrachlorophthalimide, and N-adamantyl tetrachlorophthalimide.
 8. A thermal detection system for electrical apparatus, comprising a monitor suitable for detecting smoke particles, a collecting means for removing said smoke particles for analysis and thermal particulating organic resin having a smoking temperature below 250° C. and coated on several surfaces of the electrical apparatus which has a set of at least two different chemical tags utilized on different surfaces of the electrical apparatus at a concentration in the thermal particulating organic resin coating of from about 0.01% to 0.5% and where each chemical tag can be used to readily establish the location of failure in the electrical apparatus based on the identification of the specific chemical tag within the set utilized at particular locations within the electrical apparatus by being resolved as a solvent extract of the collected organic resin smoke particles with a gas chromatograph equipped with an electron capture detector or a micro coulometric detector, where the chemical tags have a volatility within the range of a C.sub.(24-45) aliphatic paraffin, and are selected from the group consisting of(A) chemical tags capable of resisting decomposition at temperatures at least 100° C. higher than the smoking temperature of the organic resin and selected from halogenated aromatic organic compounds and polyfluorinated aliphatic organic compounds, and (B) chemical tags in the form of halogenated aromatic amic acids which are convertible to halogenated aromatic organic compounds of (A) at smoking temperatures.
 9. A thermal detection system in accordance with claim 8, where the electrical apparatus is an electric generator driven by a steam turbine.
 10. A thermal detection system in accordance with claim 8, where the electrical apparatus is an electric generator driven by a nuclear power plant.
 11. A thermal detection system in accordance with claim 8, where the electrical apparatus is an electric generator driven by a gas turbine.
 12. A thermal detection system in accordance with claim 8, where the thermal particulating organic resin is an epoxy resin.
 13. A thermal detection system in accordance with claim 8, where the chemical tags are aromatic polychlorinated organic compounds included within the formula, ##STR14## where R and R¹ together total 24-24 carbon atoms and selected from C.sub.(1-23) alkyl radicals and C.sub.(6-20) cycloalkyl radicals or the valence of the nitrogen atom can be satisfied with a heterocyclic radical having the formula, ##STR15## where Q is selected from --O--, --S-- and --SO₂ -- and y and z are integers having a value of 1 to 24 inclusive, while together totatling 12 to
 24. 14. A thermal detection system in accordance with claim 8, where the chemical tags are aromatic polychlorinated organic compounds included within the formula, ##STR16## R² and R³ are separately selected from C.sub.(1-24) alkyl radicals which together total C.sub.(12-24) carbon atoms and C.sub.(6-20) cyclo-alkyl radicals.
 15. A thermal detection system in accordance with claim 8, where the chemical tags are aromatic polychlorinated organic compounds included within the formula, ##STR17## R⁴ is selected from C.sub.(6-20) alkyl, and cycloalkyl. 